An efficient one-pot four-step domino reaction for the synthesis of C2-substituted 3-methylcyclohex-2-enones-Reference-Cited by-同舟云学术

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An efficient one-pot four-step domino reaction for the synthesis of C2-substituted 3-methylcyclohex-2-enones

Published:2010-09 Issue:39 Volume:66 Page:7856-7860
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Goncalves Sylvie,Maillos Philippe,Nicolas Marc,Wagner Alain,Baati Rachid

Funder

Laboratoire Pierre Fabre (Plantes et Industries)

CNRS

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference42 articles.

1. A NEW ROUTE TO HYDROPHENANTHRENE KETONES. THE SYNTHESIS OF THE C18 KETONE DERIVED FROM DEHYDROABIETIC ACID

2. A New Route to 2-(β-Phenylethyl)-3-methyl-Δ2-cyclohexenones1

3. A new route to benzo[a]naphthacene-8,13-diones: synthesis and revision of the structure proposed for G2N

4. Sesterterpenoids

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Cationic cyclization of keto-epoxides mediated by zirconium(IV) tetrachloride: diastereoselective synthesis of cis-decalinols;Tetrahedron;2011-10

2. Cationic Cyclization of 2-Alkenyl-1,3-dithiolanes: Diastereoselective Synthesis of trans-Decalins;The Journal of Organic Chemistry;2011-04-13

3. ChemInform Abstract: An Efficient One-Pot Four-Step Domino Reaction for the Synthesis of C2-Substituted 3-Methylcyclohex-2-enones.;ChemInform;2011-01-13

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